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Soliris
pharmaceutical product
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Statements
instance of
pharmaceutical product
1 reference
European Medicines Agency product number
EMEA/H/C/000791
reference URL
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000791/human_med_001055.jsp
retrieved
22 March 2017
mixture
1 reference
European Medicines Agency product number
EMEA/H/C/000791
reference URL
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000791/human_med_001055.jsp
retrieved
22 March 2017
has active ingredient
eculizumab
1 reference
European Medicines Agency product number
EMEA/H/C/000791
reference URL
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000791/human_med_001055.jsp
retrieved
22 March 2017
therapeutic area
paroxysmal nocturnal hemoglobinuria
authority
European Medicines Agency
start time
20 June 2007
1 reference
European Medicines Agency product number
EMEA/H/C/000791
reference URL
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000791/human_med_001055.jsp
retrieved
16 February 2017
stated in
European Medicines Agency
Identifiers
European Medicines Agency product number
EMEA/H/C/000791
1 reference
European Medicines Agency product number
EMEA/H/C/000791
reference URL
http://www.ema.europa.eu/ema/index.jsp?curl=pages/medicines/human/medicines/000791/human_med_001055.jsp
retrieved
22 March 2017
RxNorm ID
680973
0 references
PBS Drug Code
12840T
0 references
12900Y
0 references
12877R
0 references
10191J
0 references
10190H
0 references
10183Y
0 references
10525Y
0 references
12864C
0 references
12899X
0 references
12896R
0 references
10182X
0 references
10192K
0 references
10194M
0 references
10521R
0 references
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